Civco recalls eTRAX 16G needle sensors for Aurora Trackers due to potential incorrect needle tip position display on user interface. Affected units have specific part numbers and lot numbers.
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco is recalling eTR:AX 16G needle sensors for Aurora Trackers because they may show the wrong needle tip position on the device. This could lead to inaccurate medical procedures if the sensor is used during surgery.
The sensor may incorrectly identify the needle tip position on the user interface during medical procedures. This could lead to inaccurate surgical guidance if the sensor is used during procedures requiring precise needle placement.
Medical professionals using the eTRAX needle sensors for Aurora Trackers are most at risk. The recall affects specific part numbers and lot numbers produced by Civco.
Check for part number 667-158 and lot numbers A276636 or A282454 on the eTRAX 16G needle sensors for Aurora Trackers.
Verify the part number (667-158) and lot numbers (A276636 or A282454) on the eTRAX 16G needle sensor.
The recall indicates a potential for incorrect needle tip position display, which could affect surgical accuracy. However, the hazard is not described as causing serious injury in normal use.
Check for part number 667-158 and lot numbers A276636 or A282454 on the eTRAX 16G needle sensor for Aurora Trackers.
The recall does not specify a remedy, so there is no action required beyond checking if your sensor matches the affected part numbers and lot numbers.
We’ve drafted a message you can send Civco Medical Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-1737-2026 — Civco Medical Instruments Civco Medical Instruments Hello, I own a Civco Medical Instruments that is covered by recall Z-1737-2026 from Civco Medical Instruments. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
